1042966-22-2

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 469873-50-5 1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)propane-2-one 
• 2280-44-6 D-Glucose 

Downstream Products

• 1164131-42-3 (E)-1-(β-D-glucopyranosyl)-4-(4-chlorophenyl)but-3-en-2-one 
• 1432614-82-8 1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-4-(4-chlorophenyl)anthracene-9,10-dione 
• 1432614-63-5 (EE)-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-4-(4-chlorophenyl)but-1,3-diene 
• 1432615-04-7 (ZE)-1-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)-4-(4-chlorophenyl)but-1,3-diene 

Relevant academic research and scientific papers

Synthesis of C-glycosylmethyl isoxazoles via aerobic oxidation of ketoximes catalyzed by TEMPO

An efficient and high yielding synthesis of C-glycosylmethyl isoxazoles by oxidation of ketoximes in the presence of oxygen and mediated by TEMPO is described.

Synthetic studies in butenonyl C-glycosides: Preparation of polyfunctional alkanonyl glycosides and their enzyme inhibitory activity

A simple synthesis of phenyl butenoyl C-glycosides has been achieved by Aldol condensation of peracetylated glycosyl acetones with aromatic aldehydes followed by deacetylation with methanolic NaOMe. The selected butenoyl C-glycosides on conjugate addition

Aldol reaction of β-C-glycosylic ketones: synthesis of C-(E)-cinnamoyl glycosylic compounds as precursors for new biologically active C-glycosides

A series of β-C-glycosylic ketones were prepared starting from d-glucose, d-xylose, d-mannose, and cellobiose. The β-C-glycosylic ketones on aldol condensation with different aromatic aldehydes in the presence of a suitable organocatalyst led to the forma